Buprenorphine

Product NDC

0093-3601

11-digit product format

000933601

Labeler code

0093

Product ID

0093-3601_aa750280-23ed-4d6d-9666-780dab437aab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buprenorphine

Dosage form

PATCH, EXTENDED RELEASE

Route

TRANSDERMAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

NDA021306

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2017-05-30

Marketing end

2019-07-31

Substance

BUPRENORPHINE

Active strength

10 ug/h

Pharmacologic classes

Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record